Decision Date2009-10-20
Product CodeHQC
Advisory CommitteeOP
DecisionSubstantially Equivalent
Device Summary
ALCON ULTRACHOPPER is the device name listed in this FDA 510(k) record. The listed applicant is Alcon Research, Ltd.. It received FDA 510(k) clearance on 2009-10-20 under 510(k) number K091777. The device is classified under product code HQC. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the ALCON ULTRACHOPPER?
ALCON ULTRACHOPPER is a medical device that received FDA 510(k) clearance on 2009-10-20. The listed applicant is Alcon Research, Ltd.. The 510(k) number is K091777.
When did ALCON ULTRACHOPPER receive FDA 510(k) clearance?
ALCON ULTRACHOPPER received FDA 510(k) clearance on 2009-10-20, under 510(k) number K091777.
Who is the listed applicant for ALCON ULTRACHOPPER?
The FDA 510(k) record lists Alcon Research, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ALCON ULTRACHOPPER?
The FDA product code for ALCON ULTRACHOPPER is HQC.
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Official Source
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